Ünal Sedat, Varan Gamze, Benito Juan M, Aktaş Yeşim, Bilensoy Erem
Department of Pharmaceutical Technology, Faculty of Pharmacy, Erciyes University, 38280, Kayseri, Turkey.
Department of Vaccine Technology, Vaccine Institute, Hacettepe University, 06100, Ankara, Turkey.
Beilstein J Org Chem. 2023 Feb 13;19:139-157. doi: 10.3762/bjoc.19.14. eCollection 2023.
Colorectal cancer (CRC) is the third most diagnosed cancer type globally and ranks second in cancer-related deaths. With the current treatment possibilities, a definitive, safe, and effective treatment approach for CRC has not been presented yet. However, new drug delivery systems show promise in this field. Amphiphilic cyclodextrin-based nanocarriers are innovative and interesting formulation approaches for targeting the colon through oral administration. In our previous studies, oral chemotherapy for colon tumors was aimed and promising results were obtained with formulation development studies, mucin interaction, mucus penetration, cytotoxicity, and permeability in 2D cell culture, and furthermore in vivo antitumoral and antimetastatic efficacy in early and late-stage colon cancer models and biodistribution after single dose oral administration. This study was carried out to further elucidate oral camptothecin (CPT)-loaded amphiphilic cyclodextrin nanoparticles for the local treatment of colorectal tumors in terms of their drug release behavior and efficacy in 3-dimensional tumor models to predict the in vivo efficacy of different nanocarriers. The main objective was to build a bridge between formulation development and in vitro phase and animal studies. In this context, CPT-loaded polycationic-β-cyclodextrin nanoparticles caused reduced cell viability in CT26 and HT29 colon carcinoma spheroid tumors of mice and human origin, respectively. In addition, the release profile, which is one of the critical quality parameters in new drug delivery systems, was investigated mathematically by release kinetic modeling for the first time. The overall findings indicated that the strategy of orally targeting anticancer drugs such as CPT with positively charged poly-β-CD-C6 nanoparticles to colon tumors for local and/or systemic efficacy is a promising approach.
结直肠癌(CRC)是全球第三大最常被诊断出的癌症类型,在癌症相关死亡中排名第二。就目前的治疗可能性而言,尚未出现一种针对CRC的明确、安全且有效的治疗方法。然而,新型药物递送系统在这一领域显示出了前景。基于两亲性环糊精的纳米载体是通过口服给药靶向结肠的创新且有趣的制剂方法。在我们之前的研究中,针对结肠肿瘤的口服化疗是有目标的,并且通过制剂开发研究、粘蛋白相互作用、粘液渗透、细胞毒性以及二维细胞培养中的渗透性,此外还通过早期和晚期结肠癌模型中的体内抗肿瘤和抗转移功效以及单次口服给药后的生物分布,获得了有前景的结果。本研究旨在进一步阐明负载喜树碱(CPT)的两亲性环糊精纳米颗粒在三维肿瘤模型中用于结直肠肿瘤局部治疗时的药物释放行为和功效,以预测不同纳米载体的体内功效。主要目标是在制剂开发与体外阶段及动物研究之间架起一座桥梁。在此背景下,负载CPT的聚阳离子-β-环糊精纳米颗粒分别降低了小鼠和人源CT26和HT29结肠癌细胞球肿瘤中的细胞活力。此外,首次通过释放动力学建模对新药递送系统的关键质量参数之一——释放曲线进行了数学研究。总体研究结果表明,用带正电荷的聚-β-环糊精-C6纳米颗粒口服靶向CPT等抗癌药物至结肠肿瘤以实现局部和/或全身功效的策略是一种有前景的方法。